This organic molecule is dissolved in a basic aqueous solution: HO OH A short time later sensitive infrared spectroscopy reveals the presence of a new C = O stretch absorption. That is, there must now be a new molecule present with at least one C = O bond. In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule. Add/Remove step ☑

Give detailed mechanism Solution with explanation needed. Don't give Handwritten answer

please give a mechanism C C ง NH2

After running various experiments, you determine that the mechanism for the following reaction occurs in a step-wise fashion. Br + + ག ཡིག་ ཐ དང༠ པ—- ིད་ཡིག་ - དང་ ལུ ད + Using this information, draw the correct mechanism in the space below. Br Br * : ☐ ? g Add/Remove step ☑ 000 Click and drag to start drawing a structure. 18 Ar B كا

( plz do all plz and will upvote with explanation and mechanism plz give mechanism

This organic molecule is dissolved in an acidic aqueous solution: i A short time later sensitive infrared spectroscopy reveals the presence of a new C. with at least one C - OH bond. - OH stretch absorption. That is, there must now be a new molecule present In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule. : Click and drag to start drawing a structure. Add/Remove step Click and drag to start drawing a structure.

Shown below is a carbocation intermediate in an electrophilic addition reaction of HCl with an alkene. For the conformation shown, select each hydrogen whose bond to carbon is aligned for effective hyperconjugation with the vacant p orbital on the positively charged carbon. Each adjacent carbon will have only one C-H bond so aligned. • Gray = C; white = H; red = 0; blue = N; dark green = Cl; brown =Br; light green =F; purple = I; yellow = S; orange = P. • Double click to select atoms. • You can zoom in and out using the mouse scroll wheel (or pinch to zoom on touch screens).

Show the electron-flow mechanism of the following. This involves predicting major and by-products using electronic and structural effect CH3 CI. `AI C=c-H H-CI 1 %3D + + + H H. CI Br CH3 + N-Br + Br-Br = CH3 12 Br CH3 CH2 + HBr %3D 3. || I I

Give detailed mechanism Solution with explanation needed. Don't give Handwritten answer..don't copy the answer anywhere

Please provide a mechanism